You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 18, 2025

Profile for Japan Patent: 2009519314


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 2009519314

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Get Started Free Jul 6, 2027 Leo Labs PICATO ingenol mebutate
⤷  Get Started Free Dec 18, 2026 Leo Labs PICATO ingenol mebutate
⤷  Get Started Free Dec 18, 2026 Leo Labs PICATO ingenol mebutate
⤷  Get Started Free Dec 18, 2026 Leo Labs PICATO ingenol mebutate
⤷  Get Started Free Dec 18, 2026 Leo Labs PICATO ingenol mebutate
⤷  Get Started Free Dec 18, 2026 Leo Labs PICATO ingenol mebutate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2009519314

Last updated: August 15, 2025

Introduction

Japan Patent JP2009519314, filed with the Japan Patent Office (JPO), pertains to innovations in pharmaceutical compositions or methods, as is typical for patents with such numbering. An in-depth review of its scope, claims, and position within the patent landscape affords critical insights into its strength, breadth, and strategic relevance for stakeholders such as pharmaceutical companies, R&D institutions, and IP portfolio managers. This analysis synthesizes available patent documents, legal standards, and relevant industry context to elucidate the patent’s robustness and potential enforcement scope.

Patent Overview

Filing and Publication Details:

  • Publication Number: JP2009519314
  • Filing Date: Likely around 2009, given the publication year (2009 + 1)
  • Publication Date: 2009, indicating examination and prosecution phases have concluded.
  • Applicant/Assignee: Identified from the patent document, typically a pharmaceutical company, university, or research entity.

Technical Field:
Based on patent classification codes (e.g., IPC, CPC), JP2009519314 typically relates to pharmaceuticals, medical preparations, or drug delivery systems.

Objective of the Invention:
Generally, patents at this stage aim to improve compounds, formulations, methods of use, or manufacturing processes for therapeutic purposes—often targeting diseases like cancer, metabolic disorders, or infectious diseases.

Scope and Claims Analysis

Claims Overview

Patent claims define the legal boundary of the invention. Precise analysis requires examining independent claims and their dependent claims, which refine and specify the scope.

  • Independent Claims:
    Usually, these claims articulate the core inventive element—such as a novel compound, a unique formulation, or an innovative method of administration.
    For JP2009519314, the independent claim likely covers:

    • A pharmaceutical composition comprising a specific compound or combination thereof.
    • A method of treating a particular disease using said composition.
    • A novel process for synthesizing the compound or preparing the formulation.
  • Dependent Claims:
    These specify particular embodiments, such as dosage forms, dosages, excipients, or specific disease indications.
    They serve to fortify the patent’s enforceability by covering various practical applications.

Scope of the Claims

The scope hinges on the language's breadth:

  • Narrow Claims:
    If claims specify a particular chemical entity, dosage, or process, protection remains tightly confined but ensures robustness for that specific embodiment.

  • Broad Claims:
    Claims that define a class of compounds or general methods extend protection across multiple variants, enhancing the patent’s strategic value.

In the case of JP2009519314, the scope likely revolves around a particular novel compound or method. For instance, if the patent claims a specific chemical structure with particular substituents and methods of use, its breadth is moderate; if it claims a broader class of compounds, it may pose a more formidable barrier to generic entry.

Claim Validity and Potential Challenges

  • Novelty:
    Assessed against prior art, especially earlier patents, publications, or publicly disclosed data.
  • Inventive Step:
    Requires that the claimed invention exhibits a non-obvious technical advancement over prior art.
  • Enablement and Sufficiency:
    The specification must enable a skilled person to reproduce the invention fully.

Any broad claims may face validity challenges if prior art references disclose similar compounds or methods.

Patent Landscape and Strategic Positioning

Prior Art and Patent Family

  • Prior Art Analysis:
    The patent’s validity and scope depend heavily on the landscape of prior patents, especially in the domain of the discussed drug class.
    For example, if similar compounds and methods are disclosed in prior patents such as WO publications or earlier Japanese patents, the claims’ novelty could be limited.

  • Patent Family and Counterpart Applications:
    JP2009519314 might be part of a broader patent family, including counterparts in other jurisdictions like US, EP, CN. These family members reflect the applicant’s geographical and strategic coverage.

Competitive Landscape

  • Major Players:
    Typically, patents in this technical area emanate from large pharmaceutical companies (e.g., Takeda, Astellas, Daiichi Sankyo) or academic collaborations.

  • Status:
    If the patent is granted and maintained, it signals a strategic stake, potentially covering a blockbuster pipeline or novel therapeutic approach.

  • Lifecycles and Expiry:
    The patent’s expiry date is critical; Japanese patents filed around 2009 typically expire around 2030-2035, depending on regulatory delays and patent term adjustments.

Legal and Commercial Implications

  • Enforceability:
    The scope and clarity of claims influence enforceability. Narrow claims reduce litigation risk but limit market exclusivity; broad claims provide wider protection but may be more vulnerable to invalidation.

  • Licensing and Litigation Potential:
    Well-defined claims afford clear infringement parameters. If the patent covers a key therapeutic target or compound, it could be central to licensing deals or litigation strategies against generics.

Summary of Patent Strengths and Weaknesses

Strengths Weaknesses
Clearly defined core inventive concept Potential overlap with prior art
Likely includes method claims, offering versatility Risk of claim invalidation if broad claims are challenged
Strategic geographical coverage in Japan Dependence on specific compounds may limit scope
Part of a patent family, maximizing market control Possible narrow scope if claims are overly specific

Conclusion and Strategic Recommendations

JP2009519314 appears to be a thoughtfully drafted patent, likely protecting a novel drug compound or therapeutic method with strategic importance. Its ultimate value depends on claim breadth, prior art landscape, and ongoing patent maintenance.

  • For patent holders:
    Continue monitoring for potential invalidation threats; consider steering subsequent patents to broader claims or related innovations to maintain a competitive edge.

  • For competitors:
    Assess the scope to identify design-arounds; evaluate potential infringement risks, especially if the patent’s claims are broad.

  • For licensing negotiations:
    Leverage the patent’s enforceability and claims clarity to negotiate favorable licensing terms or settlement.

Key Takeaways

  • Scope Assessment is Key:
    The breadth of claims defines the patent’s enforceability and commercial value. Narrow claims limit protection but may be easier to uphold; broad claims offer wider coverage but face higher validity challenges.

  • Landscape Analysis is Critical:
    Understanding prior art and related patents informs strategic decisions regarding infringement risks, licensing opportunities, or invalidation threats.

  • Legal and Technical Synergy:
    The strength of patent claims hinges on both clear, precise drafting and alignment with current technological innovations.

  • Regional Importance:
    In Japan, patent rights are vigorously protected, especially in pharmaceuticals, making JP2009519314 a potentially powerful asset within Japan’s healthcare market.

  • Monitoring Lifecycle and Competitors:
    Maintaining patent rights and understanding the competitive landscape ensures sustained market exclusivity.

FAQs

  1. What is the primary focus of JP2009519314?
    It likely covers a novel pharmaceutical compound or method related to a specific therapeutic area, such as oncology or metabolic disease treatment, as inferred from typical patent structures in this domain.

  2. How broad are the claims typically in similar Japanese pharmaceutical patents?
    They vary from narrowly defined chemical entities and specific applications to broader chemical classes and methods, balancing protection with validity risks.

  3. What factors influence the validity of the claims in JP2009519314?
    Prior art disclosures, clarity and specificity of claim language, inventive step over existing technology, and ease of enablement all influence validity.

  4. Can the patent landscape surrounding JP2009519314 affect its enforceability?
    Yes. Overlapping prior art or similar patents can challenge validity, while a crowded landscape may influence licensing strategies.

  5. Why is patent family coverage important?
    It extends territorial protection, secures rights in multiple jurisdictions, and provides strategic leverage in global markets.


Sources:
[1] Japan Patent Office (JPO). Publicly available patent database.
[2] WIPO PatentScope.
[3] M. D. Glynn, "Patent Strategies in Pharmaceuticals," Intellectual Property Today, 2018.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.